Winocour E, Lavie V, Keshet I
J Virol. 1983 Oct;48(1):229-38. doi: 10.1128/JVI.48.1.229-238.1983.
Three simian virus (SV40)-phi X174 recombinant genomes were isolated from single BSC-1 monkey cells cotransfected with SV40 and phi X174 RF1 DNAs. The individual cell progenies were amplified, cloned, and mapped by a combination of restriction endonuclease and heteroduplex analyses. In each case, the 600 to 1,000 base pairs of phi X174 DNA (derived from different regions of the phi X174 genome) were present as single inserts, located in either the early or late SV40 regions; the deletion of SV40 DNA was greater than the size of the insert; and the remaining portions of the hybrid genome were indistinguishable from wild-type SV40 DNA, as judged by both mapping and biological tests. Hence, apart from the deletion which accommodates the phi X174 DNA insert, no other rearrangements of SV40 DNA were detected. The restriction map of a SV40-phi X174 recombinant DNA isolate before molecular cloning was indistinguishable from those of two separate cloned derivatives of that isolate, indicating that the species cloned was the major amplifiable recombinant structure generated by a single recombinant-producing cell. The relative simplicity of the SV40-phi X174 recombinant DNA examined is consistent with the notion that most recombinant-producing BSC-1 cells support single recombination events generating only one amplifiable recombinant structure.
从与猴病毒40(SV40)和噬菌体φX174 RF1 DNA共转染的单个BSC - 1猴细胞中分离出三个SV40 - φX174重组基因组。通过限制性内切酶和异源双链分析相结合的方法,对单个细胞后代进行扩增、克隆和图谱绘制。在每种情况下,600至1000个碱基对的φX174 DNA(源自φX174基因组的不同区域)以单插入片段的形式存在,位于SV40的早期或晚期区域;SV40 DNA的缺失大于插入片段的大小;通过图谱绘制和生物学测试判断,杂交基因组的其余部分与野生型SV40 DNA无法区分。因此,除了容纳φX174 DNA插入片段的缺失外,未检测到SV40 DNA的其他重排。分子克隆前的一个SV40 - φX174重组DNA分离株的限制性图谱与该分离株的两个单独克隆衍生物的图谱无法区分,这表明克隆的物种是由单个重组产生细胞产生的主要可扩增重组结构。所检测的SV40 - φX174重组DNA的相对简单性与大多数重组产生的BSC - 1细胞支持仅产生一种可扩增重组结构的单重组事件这一观点一致。